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血浆神经元特异性烯醇化酶水平作为接受吉非替尼治疗的非小细胞肺癌患者的预后标志物。

Plasma neuron-specific enolase level as a prognostic marker in patients with non-small cell lung cancer receiving gefitinib.

作者信息

Inomata Minehiko, Hayashi Ryuji, Yamamoto Azusa, Tokui Kotaro, Taka Chihiro, Okazawa Seisuke, Kambara Kenta, Suzuki Kensuke, Ichikawa Tomomi, Yamada Toru, Miwa Toshiro, Kashii Tatsuhiko, Matsui Shoko, Tobe Kazuyuki, Imura Johji

机构信息

First Department of Internal Medicine, Faculty of Medicine, University of Toyama, Toyama, Toyama 930-0194, Japan.

Department of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Toyama 930-8550, Japan.

出版信息

Mol Clin Oncol. 2015 Jul;3(4):802-806. doi: 10.3892/mco.2015.568. Epub 2015 May 14.

Abstract

Determination of the presence of epidermal growth factor receptor () gene mutation is useful for predicting the efficacy of gefitinib. However, the survival rate following the initiation of treatment with gefitinib varies among individuals. A retrospective study was conducted to investigate the associations of the pretreatment serum pro-gastrin-releasing peptide (pro-GRP) and plasma neuron-specific enolase (NSE) levels to the patient survival rate following initiation of treatment with gefitinib in non-small cell lung cancer (NSCLC) patients receiving gefitinib treatment. Patients with NSCLC harboring gene mutations who received gefitinib therapy between 2004 and 2012 were included in the study. Data from a total of 41 patients were analyzed. The serum pro-GRP level was measured in 31 patients and the plasma NSE in 22 patients. The progression-free survival (PFS) (P=0.013) and overall survival (OS) (P=0.014, log-rank test) rates decreased as the plasma NSE level increased. Statistical analysis using a Cox proportional hazards regression model adjusted for age, gender, performance status (PS) and disease stage showed that higher NSE levels were associated with shorter PFS (P=0.021) and OS (P=0.0024). By contrast, no association was detected between the serum level of pro-GRP and survival rate. The results suggest that pretreatment NSE measurement could be clinically useful in patients with NSCLC scheduled to receive gefitinib treatment.

摘要

表皮生长因子受体()基因突变的检测对于预测吉非替尼的疗效很有用。然而,开始使用吉非替尼治疗后的生存率在个体间存在差异。进行了一项回顾性研究,以调查在接受吉非替尼治疗的非小细胞肺癌(NSCLC)患者中,治疗前血清胃泌素释放肽前体(pro-GRP)和血浆神经元特异性烯醇化酶(NSE)水平与开始吉非替尼治疗后患者生存率之间的关联。纳入了2004年至2012年间接受吉非替尼治疗且携带基因突变的NSCLC患者。共分析了41例患者的数据。对31例患者检测了血清pro-GRP水平,对22例患者检测了血浆NSE水平。随着血浆NSE水平升高,无进展生存期(PFS)(P=0.013)和总生存期(OS)(P=0.014,对数秩检验)率降低。使用Cox比例风险回归模型进行的统计分析,对年龄、性别、体能状态(PS)和疾病分期进行了校正,结果显示较高的NSE水平与较短的PFS(P=0.021)和OS(P=0.0024)相关。相比之下,未检测到血清pro-GRP水平与生存率之间存在关联。结果表明,对于计划接受吉非替尼治疗的NSCLC患者,治疗前检测NSE可能具有临床意义。

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